Nickel-Catalyzed Borylative Ring-Opening Reaction of Vinylcyclopropanes with Bis(pinacolato)diboron Yielding Allylic Boronates
作者:Yuto Sumida、Hideki Yorimitsu、Koichiro Oshima
DOI:10.1021/ol801982d
日期:2008.10.16
Vinylcyclopropanes bearing one or two electron-withdrawing groups on the cyclopropane ring undergo nickel-catalyzed borylative ring opening with bis(pinacolato)diboron to yield allylic boronates. The reaction proceeded with high E selectivity.
Wilson, Stephen R.; Wiesler, Donald P., Synthetic Communications, 1980, vol. 10, # 4, p. 339 - 344
作者:Wilson, Stephen R.、Wiesler, Donald P.
DOI:——
日期:——
Improved selectivity in the preparation of some 1,1-difunctionalized 3-cyclopentenes. High yield synthesis of 3-cyclopentenecarboxylic acid